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Host association and selection on salivary protein genes in bed bugs and related blood-feeding ectoparasites
Reciprocal selective pressures can drive coevolutionary changes in parasites and hosts, and result in parasites that are highly specialized to their hosts. Selection and host co-adaptation are better understood in endoparasites than in ectoparasites, whose life cycles may be more loosely linked to t...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society Publishing
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5493930/ https://www.ncbi.nlm.nih.gov/pubmed/28680688 http://dx.doi.org/10.1098/rsos.170446 |
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author | Talbot, Benoit Balvín, Ondřej Vonhof, Maarten J. Broders, Hugh G. Fenton, Brock Keyghobadi, Nusha |
author_facet | Talbot, Benoit Balvín, Ondřej Vonhof, Maarten J. Broders, Hugh G. Fenton, Brock Keyghobadi, Nusha |
author_sort | Talbot, Benoit |
collection | PubMed |
description | Reciprocal selective pressures can drive coevolutionary changes in parasites and hosts, and result in parasites that are highly specialized to their hosts. Selection and host co-adaptation are better understood in endoparasites than in ectoparasites, whose life cycles may be more loosely linked to that of their hosts. Blood-feeding ectoparasites use salivary proteins to prevent haemostasis in the host, and maximize energy intake. Here we looked for signals of selection in salivary protein genes of ectoparasite species from a single genus (Cimex) that associate with a range of hosts including mammals (bats and humans) and birds (swallows). We analysed two genes that code for salivary proteins that inhibit platelet aggregation and vasoconstriction and may directly affect the efficiency of blood feeding in these species. Significant positive selection was detected at five codons in one gene in all bat-associated species groups. Our results suggest association with bats, versus humans or swallows, has posed a selective pressure on the salivary apyrase gene in species of Cimex. |
format | Online Article Text |
id | pubmed-5493930 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | The Royal Society Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-54939302017-07-05 Host association and selection on salivary protein genes in bed bugs and related blood-feeding ectoparasites Talbot, Benoit Balvín, Ondřej Vonhof, Maarten J. Broders, Hugh G. Fenton, Brock Keyghobadi, Nusha R Soc Open Sci Biology (Whole Organism) Reciprocal selective pressures can drive coevolutionary changes in parasites and hosts, and result in parasites that are highly specialized to their hosts. Selection and host co-adaptation are better understood in endoparasites than in ectoparasites, whose life cycles may be more loosely linked to that of their hosts. Blood-feeding ectoparasites use salivary proteins to prevent haemostasis in the host, and maximize energy intake. Here we looked for signals of selection in salivary protein genes of ectoparasite species from a single genus (Cimex) that associate with a range of hosts including mammals (bats and humans) and birds (swallows). We analysed two genes that code for salivary proteins that inhibit platelet aggregation and vasoconstriction and may directly affect the efficiency of blood feeding in these species. Significant positive selection was detected at five codons in one gene in all bat-associated species groups. Our results suggest association with bats, versus humans or swallows, has posed a selective pressure on the salivary apyrase gene in species of Cimex. The Royal Society Publishing 2017-06-21 /pmc/articles/PMC5493930/ /pubmed/28680688 http://dx.doi.org/10.1098/rsos.170446 Text en © 2017 The Authors. http://creativecommons.org/licenses/by/4.0/ Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited. |
spellingShingle | Biology (Whole Organism) Talbot, Benoit Balvín, Ondřej Vonhof, Maarten J. Broders, Hugh G. Fenton, Brock Keyghobadi, Nusha Host association and selection on salivary protein genes in bed bugs and related blood-feeding ectoparasites |
title | Host association and selection on salivary protein genes in bed bugs and related blood-feeding ectoparasites |
title_full | Host association and selection on salivary protein genes in bed bugs and related blood-feeding ectoparasites |
title_fullStr | Host association and selection on salivary protein genes in bed bugs and related blood-feeding ectoparasites |
title_full_unstemmed | Host association and selection on salivary protein genes in bed bugs and related blood-feeding ectoparasites |
title_short | Host association and selection on salivary protein genes in bed bugs and related blood-feeding ectoparasites |
title_sort | host association and selection on salivary protein genes in bed bugs and related blood-feeding ectoparasites |
topic | Biology (Whole Organism) |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5493930/ https://www.ncbi.nlm.nih.gov/pubmed/28680688 http://dx.doi.org/10.1098/rsos.170446 |
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